Evidence map›Paper›PMID 37344992›Full record

ArticleCancer science2023

Exploring olfactory receptor family 7 subfamily C member 1 as a novel oral cancer stem cell target for immunotherapy.

Sho Miyamoto, Yoshihiko Hirohashi, Rena Morita, Akihiro Miyazaki, Kazuhiro Ogi, Takayuki Kanaseki, Kentaro Ide, Jumpei Shirakawa, Tomohide Tsukahara, Aiko Murai and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Olfactory receptors and human diseases.Cell and tissue research · 2025
    Review
  7. Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 1 country.

Sho MiyamotoDepartment of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0001-9573-1161
Yoshihiko HirohashiDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0002-0608-3914
Rena MoritaDivision of Fundamental Health Sciences, School of Nursing and Social Services, Health Sciences University of Hokkaido, Tobetsu-Cho, Japan.
Akihiro MiyazakiDepartment of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Kazuhiro OgiDepartment of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Takayuki KanasekiDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0001-7294-6880
Kentaro IdeDepartment of Oral and Maxillofacial Functional Rehabilitation, Graduate School of Medicine, University of the Ryukyus, Nishihara, Japan.
Jumpei ShirakawaDepartment of Oral and Maxillofacial Functional Rehabilitation, Graduate School of Medicine, University of the Ryukyus, Nishihara, Japan.
Tomohide TsukaharaDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID https://orcid.org/0000-0002-3678-4359
Aiko MuraiDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Takashi SasayaDepartment of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Kazushige KoikeDepartment of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Shinichiro KinaCenter for Medical Education, Gunma University Graduate School of Medicine, Maebashi, Japan.ORCID https://orcid.org/0000-0002-4687-9802
Toshihiro KawanoDepartment of Oral and Maxillofacial Functional Rehabilitation, Graduate School of Medicine, University of the Ryukyus, Nishihara, Japan.
Takahiro GotoDepartment of Oral and Maxillofacial Functional Rehabilitation, Graduate School of Medicine, University of the Ryukyus, Nishihara, Japan.
Edward Hosea NtegeDepartment of Oral and Maxillofacial Functional Rehabilitation, Graduate School of Medicine, University of the Ryukyus, Nishihara, Japan.
Yusuke ShimizuDepartment of Plastic and Reconstructive Surgery, Graduate School of Medicine, University of the Ryukyus, Nishihara, Japan.
Toshihiko TorigoeDepartment of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Sapporo Medical University · JPUniversity of the Ryukyus · JPGunma University · JPHealth Sciences University of Hokkaido · JP

Funding

Japan Society for the Promotion of Science 19K10292Japan Society for the Promotion of Science 19K10337Japan Society for the Promotion of Science 20K18702
6 · The paper itself

Abstract

The mortality rate of oral cancer has not improved over the past three decades despite remarkable advances in cancer therapies. Oral cancers contain a subpopulation of cancer stem cells (CSCs) that share characteristics associated with normal stem cells, including self-renewal and multi-differentiation potential. CSCs are tumorigenic, play a critical role in cancer infiltration, recurrence, and distant metastasis, and significantly contribute to drug resistance to current therapeutic strategies, including immunotherapy. Cytotoxic CD8+ T lymphocytes (CTLs) are key immune cells that effectively recognize peptide antigens presented by the major histocompatibility complex class I molecules. Increasing evidence suggests that cancer antigen-specific targeting by CTLs effectively regulates CSCs that drive cancer progression. In this study, we utilized data from public domains and performed various bioassays on human oral squamous cell carcinoma clinical samples and cell lines, including HSC-2 and HSC-3, to investigate the potential role of olfactory receptor family 7 subfamily C member 1 (OR7C1), a seven transmembrane G-protein-coupled olfactory receptor that is also expressed in nonolfactory tissues and was previously reported as a novel marker and target of colon cancer initiating cell-targeted immunotherapy, in CSC-targeted treatment against oral cancer. We found that the OR7C1 gene was expressed only in oral CSCs, and that CTLs reacted with human leukocyte antigen-A24-restricted OR7C1 oral CSC-specific peptides. Taken together, our findings suggest that OR7C1 represents a novel target for potent CSC-targeted immunotherapy in oral cancer.

Indexed as

Carcinoma, Squamous CellMouth NeoplasmsReceptors, OdorantHumansImmunotherapyNeoplastic Stem CellsPeptidesT-Lymphocytes, CytotoxicPeptidesReceptors, Odorantcancer immunotherapycancer stem cellOR7C1oral cancerpeptide vaccine

Identifiers

PMID37344992
PMCPMC10475777
OpenAlexW4381598484

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.